MINUTE STRUCTURE OF HYBRIDS. 565 same form but of unequal length, those of their hybrid offspring have a length which corresponds approximately to the mean between the lengths in the parent- species. Thus the length of the hairs on the backs of the leaves is 0-3 mm. in Salix aurita, 12 mm. in SaUx repens, and 0-6 mm. in their hybrid Salix pUcata. The hairs in SaUx Caprea measure 0-8 mm., in SaUx viminaUs 0-3 mm., and in SaUx acuminata, their offspring, 0'5 mm. Whenever one stock is glabrous and the other hairy, one may be quite sure that the corresponding parts of their hybrid will be furnished with hairs, but less profusely than the parent-species from which that particular characteristic is derived. This is the case, for instance, with Primula Sturii, the hybrid produced by crossing the glabrous Primula minima with Pri¬ mula viUosa, which has glandular hairs. The leaves of the latter are thickly covered with these hairs, which vary from O'T mm. to 1 mm. in length, and Primula Sturii has scattered glandular hairs which measure 0'3 mm. The hybrids obtained by crossing the Purple WiUow (Salix purpurea) with the Common .Osier (Salix viminaUs) are distinguished by Botanists into two sections, one of which—Salix rubra—-approximates to the Purple Willow and the other—Salix elceagnifoUa—to the Common Osier. The leaves of the Purple Willow when mature are glabrous at the back, those of the Common Osier have small glistening hairs lying appressed to their under surfaces, paraUel to the lateral nerves, and measuring 03 mm. There are about 1800 of these hairs on a square millimetre. The hairs of the hybrid SaUx elceagnifoUa are of the same length as those of ;Si. mminalis, but there are only about 800 of them to the square miUimetre, whilst the hairs of the hybrid SaUx rubra are somewhat shorter, and there are only 400 to the square milUmetre. Recently the discovery has been made by Wettstein that the form and dis¬ position of the cells and tissues in hybrids is also a combination of the corresponding characteristics in the parent-species. The various species of the Pine genus (Pinus) may be distinguished with certainty by the anatomical structure of their needle-shaped leaves, in particular by the thickness of the epidermal cells, the number of the stone-cells lying beneath the epidermis, and the number of the resin- ducts. In the hybrids the anatomical characters of the parents in these respects are united, and the result is indeed often an exact arithmetic mean between the two. Thus a needle of the Scotch Pine (Pinus sylvestris) contains from 6 to 10 resin-ducts, that of the Mountain Pine, Pinus Mughus (montana), contains from 3 to 5, and that of the hybrid offspring of the two from 5 to 7 such ducts. The Junipers (Juniperus) afford a similar instance. In their case the leaves are dis¬ tinguished by the various thickness and length of the layer of sclerotic-cells which covers the back of each leaf, by the width of the resin-duct running through the middle of the leaf, and by the number of the cells encasing that duct. In the hybrids, such as Juniperus Kanitzii, which is produced by crossing Juniperus communis and J. sahinoides, there is evidently a union of the parental attributes in the corresponding cellular structures in the leaves. It has also been shown by Hildebrand that in the Wood-Sorrel (Oxalis) hybrids also the anatomical characters of the parents are united, but by far the most comprehensive study which has